Canonical Allele Identifier: PA111477
Gene: FGFR2 HGNC NCBI

Linked Data

ClinVar Variation Id: 374818
ClinVar RCV Id: RCV000415501 RCV001270790 RCV001591054 RCV001861462
ClinVar Variation Id: 2131381
ClinVar RCV Id: RCV003048177
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000132.3:p.Cys342Gly
CA16043910
NM_000141.5:c.1024T>G
CA2580082429
NM_000141.5:c.1023_1024delinsAG